1-Cyclopentyloctan-1-one

Base Information

Chemical Name:1-Cyclopentyloctan-1-one
CAS No.:62444-53-5
Molecular Formula:C₁₃H₂₄O
Molecular Weight:196.333
Hs Code.:
DSSTox Substance ID:DTXSID50365055
Wikidata:Q82149423
Mol file:62444-53-5.mol

Synonyms:1-cyclopentyloctan-1-one;62444-53-5;1-Octanone, 1-cyclopentyl-;starbld0043061;SCHEMBL2126939;DTXSID50365055;BBL029404;STL372774;AKOS011914533;VS-09219

Suppliers and Price of 1-Cyclopentyloctan-1-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
1-CYCLOPENTYLOCTAN-1-ONE 95.00%
5MG
$ 504.78

Total 3 raw suppliers

Chemical Property of 1-Cyclopentyloctan-1-one

Chemical Property:

PSA：17.07000
LogP:4.10620
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:7
Exact Mass:196.182715385
Heavy Atom Count:14
Complexity:157

Purity/Quality:

99% ^*data from raw suppliers

1-CYCLOPENTYLOCTAN-1-ONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCC(=O)C1CCCC1

Technology Process of 1-Cyclopentyloctan-1-one

There total 3 articles about 1-Cyclopentyloctan-1-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 38761-67-0
1-bromo-1-octyne

: 142-29-0
cyclopentene

: 62444-53-5
Cyclopentyl-n-heptylketon

Guidance literature:: With sodium hydroxide; lithium aluminium tetrahydride; monochloroborane dimethyl sulfide complex; dihydrogen peroxide;
DOI:10.1021/jo00376a041